Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:68403607 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM043027

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11981, FEVR_35

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays